ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA113607
Gene: APP
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000019724
RCV000084570
RCV003509483
ClinVar Variation:
18097
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000475.1:p.Val715Met
CA127800
NM_000484.4:c.2143G>A